A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614995



Internal ID7001884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129201205..129201905hg38UCSC Ensembl
Innerchr7:129201252..129201858hg38UCSC Ensembl
Outerchr7:129201158..129201952hg38UCSC Ensembl
chr7:128841046..128841746hg19UCSC Ensembl
Innerchr7:128841093..128841699hg19UCSC Ensembl
Outerchr7:128840999..128841793hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12966331, essv12966332, essv12966323, essv12966329, essv12966334, essv12966327, essv12966324, essv12966322, essv12966333, essv12966321, essv12966325, essv12966328, essv12966335, essv12966326, essv12966330
SamplesHG02648, HG03607, HG03667, HG03837, HG03754, HG03873, HG02733, HG01527, NA20811, HG03653, HG03598, HG02685, HG03789, HG04061, HG03989
Known GenesSMO
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614995
Frequency
Sample Size2504
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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